A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100936



Internal ID20667976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40339571..40340344hg38UCSC Ensembl
chr3:40381062..40381835hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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